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Evaluation of a colorimetric method for vitamin A estimation.
Indian Journal of Experimental Biology
|December 1, 1989
Summary
This study presents a simple, cost-effective colorimetric method for measuring plasma vitamin A. The new assay shows high correlation with established methods, offering a reliable alternative for vitamin A analysis.
Area of Science:
- Biochemistry
- Clinical Chemistry
- Analytical Chemistry
Background:
- Accurate measurement of plasma vitamin A is crucial for assessing nutritional status and diagnosing deficiencies.
- Existing spectrophotometric and spectrofluorimetric methods can be complex and require expensive equipment.
- There is a need for a simpler, more accessible method for routine vitamin A analysis.
Purpose of the Study:
- To evaluate a simple colorimetric procedure for plasma vitamin A determination.
- To compare the results of the colorimetric method with established spectrophotometric and spectrofluorimetric micro methods.
- To assess the reliability, stability, and intra-assay variation of the proposed method.
Main Methods:
- A colorimetric procedure based on the Carr-Price reaction using ferric chloride and acetyl chloride was employed.
- Vitamin A levels were determined in 30 human plasma samples and 11 rabbit liver samples.
- Results were compared against spectrophotometric and spectrofluorimetric micro methods.
Main Results:
- The colorimetric method demonstrated a high degree of correlation and good agreement with both spectrophotometric and spectrofluorimetric methods.
- Intra-assay variation was found to be 3%, which is within an acceptable range for clinical analysis.
- Reagents proved stable, allowing for sample analysis within a 4-week timeframe, unlike some alternatives.
Conclusions:
- The evaluated colorimetric procedure offers a simple, reliable, and cost-effective alternative for plasma vitamin A measurement.
- This method does not require sophisticated or expensive equipment, making it suitable for wider application.
- The stability of reagents and acceptable intra-assay variation support its utility in clinical settings.